Geochemical data from ancient sedimentary successions provide evidence for the progressive evolution of Earth's atmosphere and oceans. Key stages in increasing oxygenation are postulated for the Palaeoproterozoic era (∼2.3 billion years ago, Gyr ago) and the late Proterozoic eon (about 0.8 Gyr ago), with the latter implicated in the subsequent metazoan evolutionary expansion. In support of this rise in oxygen concentrations, a large database shows a marked change in the bacterially mediated fractionation of seawater sulphate to sulphide of Δ(34)S < 25‰ before 1 Gyr to ≥50‰ after 0.64 Gyr. This change in Δ(34)S has been interpreted to represent the evolution from single-step bacterial sulphate reduction to a combination of bacterial sulphate reduction and sulphide oxidation, largely bacterially mediated. This evolution is seen as marking the rise in atmospheric oxygen concentrations and the evolution of non-photosynthetic sulphide-oxidizing bacteria. Here we report Δ(34)S values exceeding 50‰ from a terrestrial Mesoproterozoic (1.18 Gyr old) succession in Scotland, a time period that is at present poorly characterized. This level of fractionation implies disproportionation in the sulphur cycle, probably involving sulphide-oxidizing bacteria, that is not evident from Δ(34)S data in the marine record. Disproportionation in both red beds and lacustrine black shales at our study site suggests that the Mesoproterozoic terrestrial environment was sufficiently oxygenated to support a biota that was adapted to an oxygen-rich atmosphere, but had also penetrated into subsurface sediment.

Reduction spots are common within continental red beds in the geological record. The method of formation of reduction spots is a subject of debate, but they are thought to be the result of the reducing nature of microbial life present in the sediment during burial, which caused localized reduction in sediment that was otherwise oxidized during diagenesis. Reduction spots often have dark concretionary cores commonly enriched in elements such as vanadium and uranium. This enrichment is also believed to be associated with the microbial reduction of the sediment. Isotopic data from sulphides present in the cores of analogue Triassic reduction spots are consistent with a potential microbial formation mechanism.Here we report the presence of reduction spots with vanadium-rich mica (roscoelite) -enriched cores within a terrestrial red bed sequence of the Mesoproterozoic age. These findings may be a possible indicator of life within the terrestrial geological record during the Mesoproterozoic age, a time when such evidence is otherwise very rare. These findings suggest that life had not only colonized terrestrial environments during the Mesoproterozoic age, but had established a deep biosphere in the sediment.

The McArthur River (HYC) Zn-Pb-Ag deposit in the Carpentaria Zn belt, northern Australia, is one of the world’s largest and most studied sediment-hosted base metal deposits, owing to its lack of deformation and preservation of sedimentary and ore textures. However, the ore formation process (syngenetic vs. epigenetic) is still a subject of controversy. In this paper we focus on key characteristics of the HYC deposit that remain unexplained: preservation of sedimentary carbonate (dolomite) and its association with Zn, and the role of thallium (Tl) and manganese (Mn) distribution in the orebody. Our findings demonstrate a sequence of events during ore formation: Tl is hosted almost exclusively within euhedral pyritic overgrowths around early diagenetic pyrite; sphalerite mineralization occurred after Tl-bearing pyrite overgrowths, in association with acid dissolution (replacement) of laminated and nodular dolomite across the subbasin; and outer rims are enriched in Mn on preserved dolomite at the dissolution reaction front in contact with sphalerite. New thermodynamic fluid chemistry modeling demonstrates the metal distribution and paragenesis can be explained by acidic, oxidized ore fluids entering the pyrite-dolomite host lithology, allowing reduction and pH buffering by acid carbonate dissolution, resulting in stepwise metal deposition in an evolving fluid. We argue this represents strong evidence for epigenetic ore formation at HYC. Furthermore, the primary control on ore deposition is not synsedimentary faulting in the subbasin; rather, the chemical potential of sedimentary carbonate within reduced, sulfidic lithologies appears to be of critical importance to precipitation of sphalerite.